- Trials with a EudraCT protocol (10,987)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10,987 result(s) found.
Displaying page 53 of 550.
| EudraCT Number: 2005-004652-13 | Sponsor Protocol Number: PSD502-PM-001 | Start Date*: 2006-02-01 |
| Sponsor Name:PLETHORA SOLUTIONS LIMITED | ||
| Full Title: Phase II, multi centre, randomised, double blind, placebo controlled, pilot study to determine efficacy, safety, tolerability and preliminary pharmacokinetics of PSD502 in the management of pain fr... | ||
| Medical condition: management of pain from donor sites in burns subjects undergoing skin grafts | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001386-42 | Sponsor Protocol Number: REC no:06/Q0403/25 | Start Date*: 2006-07-06 |
| Sponsor Name:Imperial College | ||
| Full Title: The timing of intra-vitreal (4mg) triamcinolone acetonide, in addition to verteporfin photodynamic therapy for choroidal neovascularisation, in age-related macular degeneration: a prospective rando... | ||
| Medical condition: Submacular choroidal neovascularisation in Age-related Macular Degeneration | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-000053-62 | Sponsor Protocol Number: sph/itu/0001 | Start Date*: 2007-06-18 | |||||||||||
| Sponsor Name:Ashford & St. Peter's Hospitals NHS Trust | |||||||||||||
| Full Title: The effects of helium-oxygen gas mixture (Heliox) on airway pressures in mechanically ventilated adult patients with acute lung injury | |||||||||||||
| Medical condition: Acute lung injury | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-000497-23 | Sponsor Protocol Number: 07/Q0703/18 | Start Date*: 2007-05-02 | ||||||||||||||||
| Sponsor Name:King's College Hospital NHS Foundation Trust [...] | ||||||||||||||||||
| Full Title: Do sulphponylureas preserve cortical function during hypoglycaemia in patients with type 1 diabetes and hypoglycaemia unawareness? | ||||||||||||||||||
| Medical condition: We are testing the hypothesis that closing the K ATP channels using sulphonylureas (glibenclamide) during experimental insulin induced hypoglycaemia can help retain cerebral function and help enhan... | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-001982-41 | Sponsor Protocol Number: RAE04 | Start Date*: 2006-10-03 | |||||||||||
| Sponsor Name:Bradford Teaching Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: An evaluation of the safety and effectiveness of combination therapy using the thiazolidinedione pioglitazone alongside insulin in type 2 diabetes mellitus. | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002208-32 | Sponsor Protocol Number: PAR06 | Start Date*: 2006-08-14 |
| Sponsor Name:York Hospital NHS Trust | ||
| Full Title: A comparison of the analgesic efficacy of oral and intravenous paracetamol (perfalgan) in a day case setting | ||
| Medical condition: We will perform a double blind randomised comparison of oral paracetamol versus intravenous paracetamol (Perfalgan) in patients undergoing knee arthroscopy in a day surgery setting. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-006761-32 | Sponsor Protocol Number: A 091152 | Start Date*: 2008-04-15 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | |||||||||||||
| Full Title: Vulval intraepithelial neoplasia: immune responses to human papillpmavirus. | |||||||||||||
| Medical condition: Vulval intraepithelial neoplasia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001571-37 | Sponsor Protocol Number: AAV2/2-hRPE65p-hRPE65 | Start Date*: 2006-12-14 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: AN OPEN-LABEL DOSE ESCALATION STUDY OF AN ADENO-ASSOCIATED VIRUS VECTOR (AAV2/2-hRPE65p-hRPE65) FOR GENE THERAPY OF SEVERE EARLY-ONSET RETINAL DEGENERATION | |||||||||||||
| Medical condition: The condition to be investigated is severe early-onset inherited retinal degeneration due to defects in the gene encoding RPE65 | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010956-93 | Sponsor Protocol Number: HM09/8885 | Start Date*: 2009-09-17 | |||||||||||
| Sponsor Name:University of Leeds [...] | |||||||||||||
| Full Title: Randomised comparisons, in myeloma patients of all ages, of thalidomide, lenalidomide, carfilzomib and bortezomib induction combinations, and of lenalidomide and combination lenalidomide vorinostat... | |||||||||||||
| Medical condition: Newly diagnosed patients with symptomatic myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-008745-38 | Sponsor Protocol Number: CKD-VitD-microcirc | Start Date*: 2009-04-08 | ||||||||||||||||
| Sponsor Name:Barts and the London NHS Trust | ||||||||||||||||||
| Full Title: THE EFFECT OF VITAMIN D ON THE MICROCIRCULATION OF PATIENTS WITH CHRONIC KIDNEY DISEASE AND VITAMIN D DEFICIENCY | ||||||||||||||||||
| Medical condition: Chronic kidney disease and vitamin D deficiency. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-006928-18 | Sponsor Protocol Number: 06/Q0603/57 | Start Date*: 2007-04-25 | |||||||||||
| Sponsor Name:Barts and The London NHS Trust | |||||||||||||
| Full Title: Randomised trial of Prontosan wound gel for prevention of exit site infection in peritoneal dialysis patients | |||||||||||||
| Medical condition: Peritoneal dialysis patients and their peritoneal dialysis catheter exit site care. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013100-32 | Sponsor Protocol Number: pms.nov.001 | Start Date*: 2009-12-01 | |||||||||||
| Sponsor Name:University of Exeter [...] | |||||||||||||
| Full Title: Does modulating the gut hormones, incretins, modify vascular function, thereby reducing the risk of vascular complications in insulin resistant individuals? | |||||||||||||
| Medical condition: Obese (BMI equal or greater than 30) individuals at a high risk of diabetes, but without overt cardiovascular disease or taking oral hypoglycaemic, anti-hypetensive or lipid lowering therapies. Pur... | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-006773-32 | Sponsor Protocol Number: HPV_CSP01 | Start Date*: 2009-05-20 | |||||||||||
| Sponsor Name:Health Protection Agency | |||||||||||||
| Full Title: A Phase IV, randomised study to evaluate the immune responses of UK adolescent girls receiving Cervarix(TM) or Gardasil(TM) Human Papillomavirus vaccines | |||||||||||||
| Medical condition: This study will investigate vaccines that prevent premalignant cervical lesions and cervical cancer causally related to Human Papillomavirus (HPV) types 16 and 18. This study will investigate wheth... | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006652-22 | Sponsor Protocol Number: AN08/8751 | Start Date*: 2009-06-03 |
| Sponsor Name:Leeds Teaching Hospital NHS Trust | ||
| Full Title: A multicentre, randomised, double blind, evaluative comparison trial of Rapydan® patch and Ametop® gel for topical anaesthesia during venous cannulation in adults admitted to hospital for day-case ... | ||
| Medical condition: ASA 1 and 2 patients admitted for Day case surgery- assessment of cannulation pain after topical anaesthetic applications. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-003327-36 | Sponsor Protocol Number: ART1 | Start Date*: 2007-01-08 |
| Sponsor Name:Guy's & St Thomas' NHS Foundation Trust [...] | ||
| Full Title: Evaluation of the efficacy of colchicine with and without betamethasone mouthwash in the management of recurrent aphthous stomatitis | ||
| Medical condition: Recurrent aphthous stomatitis (RAS) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-002653-23 | Sponsor Protocol Number: 1/07 | Start Date*: 2008-09-02 | |||||||||||
| Sponsor Name:The Police Rehabilitation Centre, Flint House | |||||||||||||
| Full Title: A pilot for a case control study to evaluate the effects of High Dosage Oxygen Therapy as an adjunct to an established program of physiotherapy and rehabilitation for sub acute soft tissue knee con... | |||||||||||||
| Medical condition: Sub acute soft tissue injuries to the knee . | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-004534-24 | Sponsor Protocol Number: 2007CV09 | Start Date*: 2008-11-18 | |||||||||||
| Sponsor Name:University of Dundee | |||||||||||||
| Full Title: Can high-dose vitamin D supplementation reduce blood pressure and markers of cardiovascular risk in older people with isolated systolic hypertension? | |||||||||||||
| Medical condition: Isolated systolic hypertension | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004897-26 | Sponsor Protocol Number: Lu-11829A | Start Date*: 2008-05-23 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: Memantine for the Long Term Management of Neuropsychiatric Symptoms in Alzheimer's disease - MAIN-AD | |||||||||||||
| Medical condition: Alzheimer's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005892-83 | Sponsor Protocol Number: WCH/2008/001 | Start Date*: 2009-01-14 |
| Sponsor Name:Epsom and St Helier University Hospitals NHS Trust | ||
| Full Title: Does metformin improve pregnancy outcomes [ incidence of LGA (≥90% birth weight centile) babies onset of maternal Gestational Diabetes, hypertension, PET, shoulder dystocia, admission to SCBU) in o... | ||
| Medical condition: Obesity in pregnancy. Obesity in pregnancy has been identified by Confidential Enquiry into Maternal And Child Health (CEMACH) (2008-2011) as a major health risk to mother and baby. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-005910-37 | Sponsor Protocol Number: MEM 1414-101 | Start Date*: 2009-02-27 | |||||||||||
| Sponsor Name:Memory Pharmaceuticals Corp | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Cross-Over Study to Evaluate the Efficacy, Safety and Tolerability of MEM 1414 (600 mg) on the Allergen-Induced Late Asthmatic Response ... | |||||||||||||
| Medical condition: Mild Allergic Asthma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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